Blood, blood-forming organs – immune system (D50-D90).
- Maxillary hemangioma – benign vascular neoplasm in the jawbone.
- Blood formation foci
Skin and subcutaneous (L00-L99)
- Cutaneous fistula
Infectious and parasitic diseases (A00-B99).
- Bacterial infection
- Viral infection
- Mycosis (fungal disease)
Mouth, esophagus (esophagus), stomach, and intestines (K00-K67; K90-K93).
- Diseases of the pulp (dental pulp)and periapical (“around the root apex”) tissues (K04)
- Acute apical periodontitis (inflammation of the periodontium (periodontium) just below the root of the tooth; apical = “toward the root of the tooth”) of pulpal origin
- Acute apical periodontitis o. n. A.
- Chronic apical periodontitis
- Apical periodontitis o. n. A.
- Apical granuloma
- Periapical granuloma
- Periapical abscess with/without fistula
- Radicular cyst
- Cyst
- Apical (periodontal)
- Periapical
- Residual
- Radicular
- Acute apical periodontitis (inflammation of the periodontium (periodontium) just below the root of the tooth; apical = “toward the root of the tooth”) of pulpal origin
- Gingivitis (inflammation of the gums) and diseases of the periodontium (K05).
- Chronic periodontitis marginalis profunda, exacerbating [acute osteomyelitis].
- Giant cell granuloma
- Cysts of the oral region, not elsewhere classified K09)
- Other diseases of the jaws (K10)
- Fibrous dysplasia
- Fibroma, ossifying
- Fibroma, non-osseous
- Ostitis round (bone inflammation)
- Phlegmon (diffuse inflammation of connective tissue that continues to spread under the skin) and abscess (encapsulated pus cavity) of the mouth.
Musculoskeletal system and connective tissue (M00-M99).
- Abacterial inflammatory bone disease [primary chronic osteomyelitis].
- SAPHO syndrome Disease from the group of forms of rheumatic diseases; the acronym SAPHO stands for the symptoms that occur:
- Synovitis (synovial inflammation; non-erosive),
- Acne (often severe conglobata form),
- Pustulosis (psoriasis of the hands and/or feet),
- Hyperostosis (bone hypertrophy; especially in the sternoclavicular joint/chest-clavicle joint).
- Osteitis (bone inflammation; spondyloarthropathy, spondylodiscitis (inflammation of the intervertebral disc and the two adjacent vertebral bodies; about 2-4% of all infectious skeletal diseases in children (mostly with Staphylococcus aureus); is predominantly caused by a hematogenous (“in the bloodstream) spread), chronic recurrent multifocal osteomyelitis (CRMO) or pustular arthroosteitis).
Neoplasms – tumor diseases (C00-D48).
- Malignant (malignant) tumors complicated by secondary bone infection [secondary chronic osteomyelitis].
- Osteosarcoma [primary chronic osteomyelitis]
- Squamous cell carcinoma, endosseous [Primary chronic osteomyelitis]
- Sclerosing bone tumors [primary chronic osteomyelitis]
- Tumor-like changes [primary chronic osteomyelitis]
- Langerhans cell histiocytoses [primary chronic, acute, and secondary chronic osteomyelitis]
- Metastases (daughter tumors) [primary chronic osteomyelitis]
- Paget’s disease – malignant neoplasia (malignant neoplasm) of the breast (breast carcinoma / breast cancer) [primary chronic osteomyelitis]
- Plasmocytoma [primary chronic osteomyelitis]
- Benign (benign) tumors, unspecified.
Injuries, poisonings, and other sequelae of external causes (S00-T98).
- Trauma to the jaw [acute osteomyelitis]
